A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606237



Internal ID16393646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12867553..12933060hg38UCSC Ensembl
Innerchr7:12907178..12972685hg19UCSC Ensembl
Innerchr7:12873703..12939210hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3865508
hg1965508
hg1865508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155296
SamplesNINDS_151
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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